Taiwan FDA registration 3c01dfdaa9c523fcd334f3010b81194a
OPPO Limb Support (Non-sterile)
TW: OPPO肢體護具 (未滅菌)
Taiwan·Risk Class 1·MD·PLUS MEDITECH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- 3c01dfdaa9c523fcd334f3010b81194a
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 004908
Company information
- Manufacturer
- PLUS MEDITECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PLUS MEDITECH CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for OPPO Limb Support (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c01dfdaa9c523fcd334f3010b81194a and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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